Rhonda Facile has over 18 years of clinical research experience including monitoring, project management, clinical outsourcing and planning, SOP development and regulatory affairs. She has participated in global process reengineering efforts in the biopharmaceutical industry as well as CRF standardization earlier in her career. She has worked for a global CRO, a global pharmaceutical company and most recently for a biotech company. She has been employed in the U.S. and most recently in Europe prior to joining CDISC. At CDISC Rhonda is CDASH Program Director, a project that seeks to standardize basic CRF data elements.